Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1841942Generated: November 3, 2026

Phenylacetaldehyde → HCID 52939283, compound

https://huagongshe.com/reaction/1841942

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenylacetaldehydeHCID 998—
ReactantTriethylamineHCID 8471—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantHCID 52938413HCID 52938413—
Solvent1,2-DichloroethaneHCID 11—
ProductHCID 52939283HCID 529392837%

Reaction Steps

To a solution of N-[4-(4-amino-piperidine-1-sulfonyl)-phenyl]-acrylamide (0.2 g, 3.1 mmol) and phenylacetaldehyde (0.06 ml, 0.52 mmol) in DCE (15 ml) was added triethylamine (0.066 ml, 0.47 mmol) in one portion. The resulting mixture was then stirred at room temperature under a nitrogen atmosphere for 30 minutes, after which time sodium triacetoxy borohydride (0.1 g, 0.47 mmol) was added portion wise. The reaction mixture was stirred at room temperature under a nitrogen atmosphere for a further 2 hours before being concentrated under vacuum. The resulting residue was purified by Prep HPLC to afford the title compound (8 mg, 7% yield) as an off-white powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08946197B2
Source datasetuspto-grants-2015_02
ORD IDord-add21eeb0ef1416d862381aa54aafc11
Source noteuspto-grants-2015_02